These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
115 related articles for article (PubMed ID: 3325588)
1. [17 alpha-hydroxylase deficiency syndrome with hyperaldosteronism. A case report]. Monno S; Furukawa K; Matsuzawa K; Furuta S Nihon Naika Gakkai Zasshi; 1987 Oct; 76(10):1565-72. PubMed ID: 3325588 [No Abstract] [Full Text] [Related]
2. A new variant of 17 alpha-hydroxylase deficiency with hyperaldosteronism in two Japanese sisters. Monno S; Takasu N Endocrinol Jpn; 1989 Apr; 36(2):315-23. PubMed ID: 2550210 [TBL] [Abstract][Full Text] [Related]
3. Primary adrenal insufficiency with hypertension. A case report on partial primary adrenal insufficiency and partial 11-beta-hydroxylase deficiency. van Deijk WA; Blom PS; VD Vijver JC Neth J Med; 1979; 22(6):191-4. PubMed ID: 316501 [No Abstract] [Full Text] [Related]
4. Hormonal profiles of heterozygotes in humans for 21-hydroxylase deficiency defined by HLA B typing. Bercovici JP; Khoury S; Le Fur JM; Saleun JP; Nahoul K; Scholler R J Steroid Biochem; 1981 Oct; 14(10):1049-54. PubMed ID: 6975398 [No Abstract] [Full Text] [Related]
5. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia. Pang S; Levine LS; Lorenzen F; Chow D; Pollack M; Dupont B; Genel M; New MI J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328 [TBL] [Abstract][Full Text] [Related]
6. [Congenital adrenogenital syndrome due to 21-hydroxylase deficiency. Pathogenesis, clinical picture, and deliberations over better therapy]. von Schnakenburg K Med Welt; 1977 Sep; 28(36):1415-22. PubMed ID: 904447 [No Abstract] [Full Text] [Related]
7. Heterozygotes for 17 alpha-hydroxylase deficiency can be detected with a short ACTH test. Wit JM; van Roermund HP; Oostdijk W; Benraad TJ; Thijssen JH; Boer P; Jansen M; Spit M; van den Brande JL Clin Endocrinol (Oxf); 1988 Jun; 28(6):657-64. PubMed ID: 2855412 [TBL] [Abstract][Full Text] [Related]
8. Mechanisms establishing the mineralocorticoid hormone patterns in the 17 alpha-hydroxylase deficiency syndrome. Biglieri EG J Steroid Biochem; 1979 Jul; 11(1B):653-7. PubMed ID: 226795 [No Abstract] [Full Text] [Related]
9. Hypertension induced by adrenocortical dysfunction--hypertension in 17 alpha-hydroxylase deficiency and metopirone-induced hypertension. Saruta T; Nakamura R; Saito I; Kondo K; Ohguro T; Yamagami K; Kitajima W; Oka M; Konishi K; Ozawa Y; Kato E; Matsuki S Jpn Circ J; 1978 May; 42(5):621-31. PubMed ID: 212619 [TBL] [Abstract][Full Text] [Related]
11. Circadian variation of plasma 17-hydroxyprogesterone among heterozygotic carriers of 21-hydroxylase deficiency (salt-losing form). Urban MD; Migeon CJ; Lee PA Horm Res; 1986; 23(2):74-7. PubMed ID: 3484712 [TBL] [Abstract][Full Text] [Related]
12. The unique patterns of plasma aldosterone and 18-hydroxycorticosterone concentrations in the 17 alpha-hydroxylase deficiency syndrome. Kater CE; Biglieri EG; Brust N; Chang B; Hirai J J Clin Endocrinol Metab; 1982 Aug; 55(2):295-302. PubMed ID: 7045152 [No Abstract] [Full Text] [Related]
13. [17-alpha-hydroxylase deficiency--a case report]. Kashiwai K; Hiraishi E; Miyashita R; Ienaga N; Murakami A Horumon To Rinsho; 1983 Jun; 31 Suppl():124-6. PubMed ID: 6604597 [No Abstract] [Full Text] [Related]
14. A case of 17 alpha-hydroxylase deficiency with special reference to the renal kallikrein-kinin system. Mita T; Shimamoto K; Ura N; Nakao T; Aoki K; Nakagawa M; Tsuzuki M; Yamazaki K; Tanaka S; Iimura O Endocrinol Jpn; 1983 Dec; 30(6):763-7. PubMed ID: 6327251 [TBL] [Abstract][Full Text] [Related]
15. No linkage between HLA and congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency. D'Armiento M; Reda G; Bisignani G; Tabolli S; Cappellaci S; Lulli P; Carbonara A; Biglieri EG N Engl J Med; 1983 Apr; 308(16):970-1. PubMed ID: 6601238 [No Abstract] [Full Text] [Related]
16. Severe hypertension with absent secondary sex characteristics due to partial deficiency of steroid 17 alpha-hydroxylase activity. Fraser R; Brown JJ; Mason PA; Morton JJ; Lever AF; Robertson JI; Lee HA; Miller H J Hum Hypertens; 1987 Jun; 1(1):53-8. PubMed ID: 2854163 [TBL] [Abstract][Full Text] [Related]
17. Effect of hydrocortisone dose schedule on adrenal steroid secretion in congenital adrenal hyperplasia. Winterer J; Chrousos GP; Loriaux DL; Cutler GB Ann N Y Acad Sci; 1985; 458():182-92. PubMed ID: 3879121 [No Abstract] [Full Text] [Related]
18. A female pseudohermaphrodite with salt losing congenital adrenal hyperplasia as the result of 21--beta--OH deficiency. Preeyasombat C; Siripoonya P; Tejavej A; Pitchayayothin N J Med Assoc Thai; 1975 Mar; 58(3):61-9. PubMed ID: 1127377 [No Abstract] [Full Text] [Related]
19. Clinical and endocrinological aspects of 21-hydroxylase deficiency. New MI Ann N Y Acad Sci; 1985; 458():1-27. PubMed ID: 3911845 [No Abstract] [Full Text] [Related]
20. [Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. A clinical case]. ZacharÃas S; Contreras P Rev Chil Obstet Ginecol; 1984; 49(5):295-9. PubMed ID: 6242254 [No Abstract] [Full Text] [Related] [Next] [New Search]